Canonical Allele Identifier: CA1621887787

Gene: MDGA1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.37653000G= , CM000668.2:g.37653000G=	GRCh38
NC_000006.11:g.37620776G= , CM000668.1:g.37620776G=	GRCh37
NC_000006.10:g.37728754G=	NCBI36
NG_051764.1:g.49991C=

Transcript Alleles

HGVS	Amino-acid Change
NM_153487.4:c.983-660C= MANE Select	NP_705691.1:n.983-660C=
ENST00000434837.8:c.983-660C= MANE Select	ENSP00000402584.2:n.983-660C=
NM_153487.3:c.983-660C=	NP_705691.1:n.983-660C=
ENST00000434837.7:c.983-660C=	ENSP00000402584.2:n.983-660C=
ENST00000478143.2:n.1566-660C=
ENST00000505425.5:c.983-660C=	ENSP00000422042.1:n.983-660C=
ENST00000650466.1:c.983-660C=	ENSP00000498018.1:n.983-660C=
ENST00000681439.1:c.215-660C=	ENSP00000506441.1:n.215-660C=
ENST00000681472.1:c.983-660C=	ENSP00000506519.1:n.983-660C=
XM_006715056.2:c.983-660C=	XP_006715119.1:n.983-660C=
XM_006715056.3:c.983-660C=	XP_006715119.1:n.983-660C=
XM_006715057.2:c.983-660C=	XP_006715120.1:n.983-660C=
XM_017010734.1:c.983-660C=	XP_016866223.1:n.983-660C=
XR_926140.1:n.1172-660C=
XR_926140.2:n.1106-660C=
XR_926141.1:n.1172-660C=
XR_926141.2:n.1106-660C=
XR_926142.1:n.1172-660C=
XR_926142.2:n.1106-660C=